Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Heptyl acetate | HCID 8159 | — |
| Reactant | Hexafluoropropylene | HCID 8302 | — |
| Reactant | Fluorine | HCID 24524 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | HCID 86758092 | HCID 86758092 | — |
| Solvent | Diglyme | HCID 8150 | — |
| Product | HCID 12654515 | HCID 12654515 | — |
Reaction Steps
A mixture consisting of 2027 g of trifluoroacetic acid pentadecafluoroheptyl ester (made by reacting heptyl acetate with fluorine gas as described in U.S. Pat. No. 5,399,718 (Costello et al.)), 777 g of 3M™ PF-5052 Performance Liquid (a mixture of perfluorinated solvents, available from 3M Company), 3171 g of anhydrous diglyme and 79 g of anhydrous potassium fluoride were added to a 2-gallon (7.6 L) stainless steel stirred pressure vessel. The vessel was heated and 1816 g of hexafluoropropylene was added over a 2-hour period while maintaining a reaction temperature of about 50° C. The vessel was held at 50° C. for an additional 1½ hours after the hexafluoropropylene addition was complete. The reactor was cooled and drained. The resulting liquid was phase split and the lower phase fractionally distilled to give 565 g of 1,1,1,2,4,4,4-heptafluoro-3-trifluoromethyl-butan-2-one having a boiling point of 25° C. and purity of 95% and 1427 g of 1,1,1,2,4,4,5,5,6,6,7,7,8,8,9,9,9-heptadecafluoro-2-trifluoromethyl-nonan-3-one, having a boiling point of 134° C. and a 98.5% purity as determined by gas chromatography and mass spectroscopy.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06403149B1 |
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| Source dataset | uspto-grants-2002_06 |
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| ORD ID | ord-00460807e8614b7b92b607a0e21cf453 |
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| Source note | uspto-grants-2002_06 |
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